VivaGuard Lancets (30G) VGL01-383

GUDID 00840423500110

VivaGuard Lancets (30G)

ABOUND Diagnostics, Inc.

Blood lancet, single-use

• Primary Device ID: 00840423500110
• NIH Device Record Key: f6712c8f-db53-4d70-b1d7-c59b754f3689
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VivaGuard Lancets (30G)
• Version Model Number: VGL01-383
• Catalog Number: VGL01-383
• Company DUNS: 119217208
• Company Name: ABOUND Diagnostics, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com
• Phone: 8889696928
• Email: lmariano@abounddiagnostics.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840423500110 [Primary]
GS1	00840423500387 [Package]; Package: Carton [200 Units]; In Commercial Distribution

FDA Product Code

• FMK: Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-04-21
• Device Publish Date: 2025-04-11

Devices Manufactured by ABOUND Diagnostics, Inc.

• 00840423500516 - VivaGuard Lancets (21G): 2025-04-21 VivaGuard Lancets (21G)
• 00840423500509 - VivaGuard Lancets (23G): 2025-04-21 VivaGuard Lancets (23G)
• 00840423500400 - VivaGuard Lancets (26G): 2025-04-21 VivaGuard Lancets (26G)
• 00840423500103 - VivaGuard Lancets (28G): 2025-04-21 VivaGuard Lancets (28G)
• 00840423500110 - VivaGuard Lancets (30G): 2025-04-21VivaGuard Lancets (30G)
• 00840423500110 - VivaGuard Lancets (30G): 2025-04-21 VivaGuard Lancets (30G)
• 00840423500424 - VivaGuard Lancing Device: 2025-04-21 VivaGuard Lancing Device
• 00840423500486 - VivaGuard Safety Lancets (18G): 2025-04-21 VivaGuard Safety Lancets (18G)
• 00840423500158 - VivaGuard Safety Lancets (21G): 2025-04-21 VivaGuard Safety Lancets (21G)